PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome-Reference-Cited by-同舟云学术

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Published:2012-01 Issue:1 Volume:90 Page:152-160
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Heron Sarah E.,Grinton Bronwyn E.,Kivity Sara,Afawi Zaid,Zuberi Sameer M.,Hughes James N.,Pridmore Clair,Hodgson Bree L.,Iona Xenia,Sadleir Lynette G.,Pelekanos James,Herlenius Eric,Goldberg-Stern Hadassa,Bassan Haim,Haan Eric,Korczyn Amos D.,Gardner Alison E.,Corbett Mark A.,Gécz Jozef,Thomas Paul Q.,Mulley John C.,Berkovic Samuel F.,Scheffer Ingrid E.,Dibbens Leanne M.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference26 articles.

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2. A novel genetic locus for benign familial infantile seizures maps to chromosome 1p36.12-p35.1;Li;Clin. Genet.,2008

3. Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome;Caraballo;Am. J. Hum. Genet.,2001

4. Benign familial infantile convulsions: Linkage to chromosome 16p12-q12 in 14 families;Weber;Epilepsia,2004

5. Refinement of the chromosome 16 locus for benign familial infantile convulsions;Callenbach;Clin. Genet.,2005

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